Proguanil Hydrochloride

CHEMBL1201059 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
290.2 g/mol
LogP
Phase
4

Proguanil hydrochloride is the hydrochloride salt form of proguanil, an antimalarial biguanide prodrug converted to cycloguanil, a dihydrofolate reductase inhibitor active against Plasmodium species. See proguanil for complete pharmacological details.

Peso molecular

290,1900 g/mol

TPSA

88,80 Ų

Áreas terapéuticas

Mecanismo de acción

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Estructura 2D

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SMILES

CC(C)NC(=N)NC(=N)Nc1ccc(Cl)cc1.Cl

InChI

InChI=1S/C11H16ClN5.ClH/c1-7(2)15-10(13)17-11(14)16-9-5-3-8(12)4-6-9;/h3-7H,1-2H3,(H5,13,14,15,16,17);1H

Molecular Formula

C11H17Cl2N5

HBD / HBA

4 / 1

Enlaces Rotables

4

Átomos Pesados

18

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Preguntas frecuentes

Proguanil hydrochloride is the hydrochloride salt form of proguanil, an antimalarial biguanide prodrug converted to cycloguanil, a dihydrofolate reductase inhibitor active against Plasmodium species. See proguanil for complete pharmacological details.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Proguanil Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201059. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9570076. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso médico

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.